Run ID: ERR751332
Sample name:
Date: 02-04-2023 04:25:06
Number of reads: 3424866
Percentage reads mapped: 68.65
Strain: lineage6.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage6 | West-Africa 2 | AFRI_1 | RD702 | 1.0 |
lineage6.2 | West-Africa 2 | AFRI_1 | RD702 | 1.0 |
lineage6.2.1 | West-Africa 2 | AFRI_1 | RD702 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5072 | c.-168G>T | upstream_gene_variant | 1.0 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8493 | p.Leu398Phe | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491668 | p.Lys296Glu | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 760969 | p.Ser388Leu | missense_variant | 1.0 |
rpoB | 761723 | p.Glu639Asp | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.99 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1303149 | c.219C>T | synonymous_variant | 0.99 |
Rv1258c | 1406685 | p.Val219Ala | missense_variant | 1.0 |
embR | 1416633 | p.Leu239Val | missense_variant | 1.0 |
atpE | 1461251 | c.207G>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472266 | n.421C>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472715 | n.870C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472770 | n.925C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472812 | n.967A>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476336 | n.2679C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476356 | n.2699C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476357 | n.2700T>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476428 | n.2771C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476501 | n.2844C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.14 |
inhA | 1674434 | p.Val78Ala | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918588 | p.Glu217Lys | missense_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ahpC | 2726556 | p.Ala122Thr | missense_variant | 0.99 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3612800 | p.Val106Ala | missense_variant | 1.0 |
alr | 3840559 | p.Arg288Ser | missense_variant | 1.0 |
alr | 3840618 | p.Asp268Gly | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241843 | p.Leu661Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243541 | c.309C>T | synonymous_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embA | 4244379 | p.Pro383Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269522 | c.-686C>T | upstream_gene_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326465 | p.Ile337Val | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |